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Baccharis tola

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fd251c12a0026741076
Scientific name Baccharis tola
Authority Phil.
First published in Fl. Atacam. : 30 (1860)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Baccharis tola subsp. altiplanicolia F.H.Hellw. Mitt. Bot. Staatssamml. München 29: 333 (1990)
Baccharis tola subsp. fimbriata Joch.Müll. Syst. Bot. Monogr. 76: 97 (-99; figs. 32-33) (2006)
Baccharis tola subsp. tola Fl. Atacam. 30 (1860)

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Southern South America
      • Argentina Northwest
      • Chile North
    • Western South America
      • Bolivia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000122613
Tropicos 2704910
KEW urn:lsid:ipni.org:names:273051-2
Open Tree Of Life 7051199
Observations.org 292300
NCBI Taxonomy 2528738
IPNI 273051-2
iNaturalist 842217
GBIF 7338486

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Exploring the leishmanicidal potential of terpenoids: a comprehensive review on mechanisms of cell death Rodrigues AC, Carloto AC, Gonçalves MD, Concato VM, Detoni MB, dos Santos YM, Cruz EM, Madureira MB, Nunes AP, Pires MF, Santos NC, Marques RE, Bidoia DL, Borges Figueiredo F, Pavanelli WR Front Cell Infect Microbiol 19-Sep-2023
PMCID:PMC10550302
doi:10.3389/fcimb.2023.1260448
PMID:37799331
Antimicrobial Diterpenes: Recent Development From Natural Sources Saha P, Rahman FI, Hussain F, Rahman SM, Rahman MM Front Pharmacol 28-Feb-2022
PMCID:PMC8918777
doi:10.3389/fphar.2021.820312
PMID:35295739
The Search for Putative Hits in Combating Leishmaniasis: The Contributions of Natural Products Over the Last Decade Sakyi PO, Amewu RK, Devine RN, Ismaila E, Miller WA, Kwofie SK Nat Prod Bioprospect 14-Jul-2021
PMCID:PMC8279035
doi:10.1007/s13659-021-00311-2
PMID:34260050
Intoxication by Astragalus garbancillo var. garbancillo in llamas Marin RE, Micheloud JF, Vignale ND, Gimeno EJ, O’Toole D, Gardner DR, Woods L, Uzal FA J Vet Diagn Invest 01-Apr-2020
PMCID:PMC7377608
doi:10.1177/1040638720914338
PMID:32233843
Structural Elucidation and Antimicrobial Characterization of Novel Diterpenoids from Fabiana densa var. ramulosa Quaglio D, Corradi S, Erazo S, Vergine V, Berardozzi S, Sciubba F, Cappiello F, Crestoni ME, Ascenzioni F, Imperi F, Delle Monache F, Mori M, Loffredo MR, Ghirga F, Casciaro B, Botta B, Mangoni ML ACS Med Chem Lett 30-Jan-2020
PMCID:PMC7236223
doi:10.1021/acsmedchemlett.9b00605
PMID:32435382
Nitrogen cycling in an extreme hyperarid environment inferred from δ15N analyses of plants, soils and herbivore diet Díaz FP, Frugone M, Gutiérrez RA, Latorre C Sci Rep 09-Mar-2016
PMCID:PMC4783660
doi:10.1038/srep22226
PMID:26956399
Subject Index N/A 01-Jan-2005
PMCID:PMC7148952
doi:10.1016/S1572-5995(05)80049-3
Diterpenoids from Baccharis tola Aurelio San Martín, Juana Rovirosa, Rodolfo Becker, Mariano Castillo Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)83018-4
Diterpenoids from Baccharis tola Aurelio San Martín, Juana Rovirosa, Mariano Castillo Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84036-4

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(8R,13S)-13-Methyl-17-norkaur-15-en-18-ol 500043 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C=C2)(C)CO)C 288.50 unknown https://doi.org/10.1016/S0031-9422(00)84036-4
https://doi.org/10.1016/0031-9422(80)83018-4
[(1R,4S,5R,9S,10S,13S)-5,9,13-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methanol 22210606 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C=C2)(C)CO)C 288.50 unknown https://doi.org/10.1016/0031-9422(80)83018-4
[(1R,4S,5S,9S,10S,13S)-5,9,13-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methanol 122180687 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C=C2)(C)CO)C 288.50 unknown https://doi.org/10.1016/0031-9422(80)83018-4
[(1R,4S,9S,10S,13S)-5-(acetyloxymethyl)-9,13-dimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methyl acetate 162891781 Click to see CC(=O)OCC1(CCCC2(C1CCC34C2CCC(C3)(C=C4)C)C)COC(=O)C 388.50 unknown https://doi.org/10.1016/S0031-9422(00)84036-4
[5-(Acetyloxymethyl)-9,13-dimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methyl acetate 162891780 Click to see CC(=O)OCC1(CCCC2(C1CCC34C2CCC(C3)(C=C4)C)C)COC(=O)C 388.50 unknown https://doi.org/10.1016/S0031-9422(00)84036-4
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,4aR,6aR,7S,10aS,10bR)-3-ethenyl-3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-7-yl]methanol 101665405 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)CO 306.50 unknown https://doi.org/10.1016/0031-9422(80)83018-4
19-Hydroxy-13-epimanoyl oxide 626002 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)CO 306.50 unknown https://doi.org/10.1016/0031-9422(80)83018-4
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/0031-9422(80)83018-4
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/0031-9422(80)83018-4
https://doi.org/10.1016/S0031-9422(00)84036-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetovanillone 2214 Click to see CC(=O)C1=CC(=C(C=C1)O)OC 166.17 unknown https://doi.org/10.1016/S0031-9422(00)84036-4
https://doi.org/10.1016/0031-9422(80)83018-4
> Organoheterocyclic compounds / Oxanes
(5,9,13-Trimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-5-yl)methanol 74034169 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C5C2O5)(C)CO)C 304.50 unknown https://doi.org/10.1016/0031-9422(80)83018-4
https://doi.org/10.1016/S0031-9422(00)84036-4
[(1S,4S,5R,9R,10S,13S,14S,16R)-5,9,13-trimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-5-yl]methanol 155514811 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C5C2O5)(C)CO)C 304.50 unknown https://doi.org/10.1016/0031-9422(80)83018-4
[(1S,4S,5S,9R,10S,13S,14R,16S)-5,9,13-trimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-5-yl]methanol 23252733 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C5C2O5)(C)CO)C 304.50 unknown https://doi.org/10.1016/S0031-9422(00)84036-4
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/S0031-9422(00)84036-4
https://doi.org/10.1016/0031-9422(80)83018-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Apigenin 7,4'-dimethyl ether 5281601 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 unknown https://doi.org/10.1016/S0031-9422(00)84036-4

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